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Impact of toll-like receptor 4 variations on nasopharyngeal carcinoma risk and survival in tunisian population.
Ben Chaaben, Arij; Ayadi, Imen; Abaza, Hejer; Baroudi, Olfa; Douik, Hayet; Harzallah, Latifa; Bouassida, Jihen; Bouckouaci, Wahid; Guemira, Fethi; Mankai, Amani; Kharrat, Maher; Tamouza, Ryad.
Affiliation
  • Ben Chaaben A; Humain genetic lab, Medical school of Tunis, Tunis El Manar University, Tunisia.
  • Ayadi I; Clinical biology lab, Salah Azaiz Institute, Tunisia.
  • Abaza H; High school of sciences and techniques of health, Tunis El Manar University, Tunisia.
  • Baroudi O; Immunology laboratory, La Rabta hospital, Tunis, Tunisia.
  • Douik H; Humain genetic lab, Medical school of Tunis, Tunis El Manar University, Tunisia.
  • Harzallah L; Clinical biology lab, Salah Azaiz Institute, Tunisia.
  • Bouassida J; Humain genetic lab, Medical school of Tunis, Tunis El Manar University, Tunisia.
  • Bouckouaci W; Humain genetic lab, Medical school of Tunis, Tunis El Manar University, Tunisia.
  • Guemira F; Clinical biology lab, Salah Azaiz Institute, Tunisia.
  • Mankai A; Clinical biology lab, Salah Azaiz Institute, Tunisia.
  • Kharrat M; University Paris Est Créteil, INSERM, IMRB, Translational Neuropsychiatry, AP-HP, DMU IMPACT, FHU ADAPT, Fondation Fonda Mental, Créteil, France.
  • Tamouza R; University Paris Est Créteil, INSERM, IMRB, Translational Neuropsychiatry, AP-HP, DMU IMPACT, FHU ADAPT, Fondation Fonda Mental, Créteil, France.
Tunis Med ; 102(2): 100-106, 2024 Feb 05.
Article in En | MEDLINE | ID: mdl-38567476
ABSTRACT

INTRODUCTION:

The Toll-like receptor 4 (TLR4), an important member of the host's innate immune response, is coded by a polymorphic gene. This polymorphism could be a predisposing factor for NasoPharyngeal Carcinoma (NPC).

AIM:

To determine the association between TLR4 gene polymorphisms and the susceptibility to NPC in a cohort of Tunisian affected patients.

METHODS:

Genomic DNAs from 245 unrelated patients affected by undifferentiated carcinoma type (UCNT) and 264 unrelated healthy controls were genotyped for the five single nucleotides polymorphisms (SNPs) of TLR4 locus (4434 A>G (rs1927914),7263 G>C (rs10759932), 6134 A>G(rs4986790), 8851C>T (rs 4986791), 5272 T>C(rs11536889), +8469 T>C (rs11536891)) by Taqman® 5'-nuclease assay.

RESULTS:

Among all polymorphisms studied, only the rs4986790 G and rs4986791 T alleles were significantly more prevalent in patients' group than controls (45% vs. 38%; p=0.03; pc=0.06) and increased the risk of the NPC (OR=1.3, 95% CI=1.01-1.69). Also, we found that the frequency of the rs4986790 AA and rs4986791 TT genotypes was significantly higher in controls than in patients (25.7% vs 37%; p=0.006, pc=0.02) and conferred a protector factor in NPC (OR= 0.59, 95% CI= 0.39-0.87). Further, based on the Kaplan-Meier survival curve we observed also the positive effect ofrs1927914 AA genotype on a prognostic of NPC (p=0.006; pc=0.01).

CONCLUSION:

Our study demonstrated that impaired production of TLR4 seems to be a risk factor of NPC development but functional studies are needed to confirm these findings. As to rs1927914 AA appears to be a good biomarker for better survival in a patient with NPC.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Nasopharyngeal Neoplasms / Genetic Predisposition to Disease Limits: Humans Language: En Journal: La tunisie med / La tunisie medicale / Tunis Med Year: 2024 Document type: Article Affiliation country: Túnez Country of publication: Túnez

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Nasopharyngeal Neoplasms / Genetic Predisposition to Disease Limits: Humans Language: En Journal: La tunisie med / La tunisie medicale / Tunis Med Year: 2024 Document type: Article Affiliation country: Túnez Country of publication: Túnez